MeSH Browser

MeSH Supplementary: hemoglobin Görwihl
Unique ID: C470779
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C470779
Entry Term(s): Hb Görwihl
Registry Numbers: 0
Heading Mapped to: *Hemoglobins, Abnormal
Frequency: 3
Note: has the mutation (alpha2beta(2)5(A2)Pro to Ala), an electrophoretically silent variant with impaired glycation
Source: Clin Chem 2003 Jan;49(1):137-43
Date of Entry: 2003/02/03
Revision Date: 1955/01/01

hemoglobin Görwihl MeSH Supplementary Concept Data 2025